Protein name: RhAG Aliases: RHAG (Rh50A) Substrates: NH4+, NH3 Transport type: H+ Tissue and cellular expression: red blood cells Subcellular expression: cell membrane Disease: Rhnull-regulator, Rhmod, OHSt Locus: 6p12.3 Sequence ID: NP_000315.2, NM_000324.2 Gene ID: 6005 Splice variants: N/D


Gene names: RHAG, RH50
Protein names and data: RHAG_HUMAN, Full=Ammonium transporter Rh type A, Full=Erythrocyte membrane glycoprotein Rh50;Full=Erythrocyte plasma membrane 50 kDa glycoprotein;Short=Rh50A;Full=Rhesus blood group family type A glycoprotein;Short=Rh family type A glycoprotein;Short=Rh type A glycoprotein;Full=Rhesus blood group-associated ammonia channel;Full=Rhesus blood group-associated glycoprotein;CD_antigen=CD241; Length: 409 a.a., Mass: 44198 Da,
fasta formatted sequence

Function: Associated with rhesus blood group antigen expression. May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane
Cellular location: Membrane; Multi-pass membrane protein
Tissue specificity: Erythrocytes

Database cross-references

UniProt: Q02094
NextBio: 23423
OMIM: 180297 268150
Ensembl: ENST00000371175
GeneCard: GC06M049680
TCDB: 1.A.11.4.3
Guide to Pharmacology: SLC42A1 (1198)
SLC42 family of Rhesus glycoprotein ammonium transporters (1198)

HGNC: HGNC:10006

Genetic variants

See also Ensembl:ENST00000371175